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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 15488

FusionGeneSummary for GRN_TMEM54

check button Fusion gene summary
Fusion gene informationFusion gene name: GRN_TMEM54
Fusion gene ID: 15488
HgeneTgene
Gene symbol

GRN

TMEM54

Gene ID

2896

113452

Gene namegranulin precursortransmembrane protein 54
SynonymsCLN11|GEP|GP88|PCDGF|PEPI|PGRNBCLP|CAC-1|CAC1
Cytomap

17q21.31

1p35.1

Type of geneprotein-codingprotein-coding
DescriptiongranulinsPC cell-derived growth factoracrograningranulin-epithelinproepithelinprogranulintransmembrane protein 54beta-casein-like proteinprotein CAC-1
Modification date2018052220180519
UniProtAcc

P28799

Q969K7

Ensembl transtripts involved in fusion geneENST00000053867, ENST00000589265, 
ENST00000589923, 
ENST00000373463, 
ENST00000329151, ENST00000475208, 
Fusion gene scores* DoF score13 X 10 X 6=7801 X 1 X 1=1
# samples 192
** MAII scorelog2(19/780*10)=-2.03747470541866
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/1*10)=4.32192809488736
Context

PubMed: GRN [Title/Abstract] AND TMEM54 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID

check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1AW062631GRNchr17

42428455

-TMEM54chr1

33361292

+
ChiTaRS3.1AW062637GRNchr17

42428455

-TMEM54chr1

33361292

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000053867ENST00000373463GRNchr17

42428455

-TMEM54chr1

33361292

+
5CDS-intronENST00000053867ENST00000329151GRNchr17

42428455

-TMEM54chr1

33361292

+
5CDS-5UTRENST00000053867ENST00000475208GRNchr17

42428455

-TMEM54chr1

33361292

+
intron-3CDSENST00000589265ENST00000373463GRNchr17

42428455

-TMEM54chr1

33361292

+
intron-intronENST00000589265ENST00000329151GRNchr17

42428455

-TMEM54chr1

33361292

+
intron-5UTRENST00000589265ENST00000475208GRNchr17

42428455

-TMEM54chr1

33361292

+
3UTR-3CDSENST00000589923ENST00000373463GRNchr17

42428455

-TMEM54chr1

33361292

+
3UTR-intronENST00000589923ENST00000329151GRNchr17

42428455

-TMEM54chr1

33361292

+
3UTR-5UTRENST00000589923ENST00000475208GRNchr17

42428455

-TMEM54chr1

33361292

+

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FusionProtFeatures for GRN_TMEM54


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GRN

P28799

TMEM54

Q969K7


check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

.

* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for GRN_TMEM54


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for GRN_TMEM54


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for GRN_TMEM54


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for GRN_TMEM54


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGRNC0011570Mental Depression3PSYGENET
HgeneGRNC0011581Depressive disorder3HPO;PSYGENET
HgeneGRNC0005586Bipolar Disorder2PSYGENET
HgeneGRNC0036341Schizophrenia2PSYGENET
HgeneGRNC0338451Frontotemporal dementia2CTD_human;HPO
HgeneGRNC0497327Dementia2CTD_human
HgeneGRNC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneGRNC0027746Nerve Degeneration1CTD_human
HgeneGRNC0751072Frontotemporal Lobar Degeneration1CTD_human
HgeneGRNC1843792FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED1CTD_human;UNIPROT